WormBase Tree Display for Variation: WBVar02126289

WBVar02126289 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h10727
    Other_name: F47G6.4b.1:c.486-2212C>T
      F47G6.4a.1:c.2517-2212C>T
    HGVSg: CHROMOSOME_I:g.1458017C>T
  Sequence_details: SMap: S_parent: Sequence: F47G6
    Flanking_sequences: TAATTTAAATTTTTTTATAACATCACACGGGGTTCTGGCC TCCTCATTGAATTTTTCGCGCTCCATTGACAATCGCCTGCCGGGCGGGAAAGTCGTGTACTCCACACGGACAAATACATT
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 1458018 1458018
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023787
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00004969
    Transcript: F47G6.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47G6.4a.1:c.2517-2212C>T
        Intron_number: 11/19
      F47G6.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47G6.4b.1:c.486-2212C>T
        Intron_number: 3/10
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose